ISSN:
1432-198X
Schlagwort(e):
Key words: Acrorenal syndrome
;
Oligomeganephronia
;
Limb defects
;
Pigmentary retinopathy
;
Renal failure
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Medizin
Notizen:
Abstract. The clinical, biochemical, radiological, and histological data of a 5-year-old boy with severe limb deformities and renal failure due to oligomeganephronia and renal hypoplasia are reported. This patient represents another example of acrorenal syndrome. This boy has a severe visual defect due to pigmentory retinopathy, which has not been reported previously.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/s004670050211
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